Sr. Supervisor, Manufacturing

Genentech • Oceanside, CA

28d • Onsite

About The Position

As a Senior Manufacturing Supervisor, you will lead a high-performing team to produce and deliver quality products for patients around the world. We are a 24/7 site that operates in a fast-paced, compliance-driven environment where safety, collaboration, and operational excellence are top priorities. In this role, you'll oversee daily floor operations, coach and develop staff, and drive continuous improvement across manufacturing processes that support the production of critical products. This is a unique opportunity to lead with impact, support innovation, and shape the future of a world-class commercial manufacturing organization.

Requirements

• Proficiency in the English language- reading, writing, and communication.
• Possess thorough knowledge and understanding of cGMPs and familiarity with FDA guidelines. Familiarity with ICH and European guidelines.
• Demonstrate organizational, time management, delegation and leadership skills to achieve successful results.
• Must be able to work all shifts, required overtime as needed, and stand for extended periods of time.
• Must be able to interface with computer systems to successfully operate manufacturing equipment. Experience with distributed control systems or other manufacturing automation is preferred.
• Must be able to successfully pass all job-related tests and certifications required for working in a cGMP quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job.
• Must re-qualify every year on all job-related training and certifications as job or qualifications require.
• May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility. Lifting up to 25lbs may be required. The cleanroom environment requires that company provided gowning is worn. This may include plant uniform, coveralls, gloves and safety shoes. Additionally, regulations prohibit makeup, jewelry, and other personal items from entering the clean room environment.
• Bachelor's degree with 7+ years industry experience or Master's degree with 5+ years industry experience (scientific and technical degrees preferred, e.g. Life Science or Engineering)
• 2 years in supervisory role

Nice To Haves

• Experience with biologics manufacturing is preferred.
• Hardworking and fast learning individual that thrives in a high paced environment
• Experience in clean room environment and familiarity with cGMP and ISO/FDA standards is strongly preferred
• Ability to think critically and work both tactically and strategically
• Exhibit creativity in adapting to situations, develop contingency plans, and make decisions
• Strong quality mindset with attention to detail and a desire to deliver service excellence
• Ability to work effectively with others, exhibiting a professional manner and establish constructive working relationships
• Experience in a GMP working environment with Background in Cell Culture/Purification is highly desired

Responsibilities

• Coordinate, lead and supervise daily operations of a designated manufacturing group.
• Ensure maintenance of a safe manufacturing work environment that complies with company and state regulations. Ensure that all employees are trained in safety practices for their assigned job tasks.
• Have responsibility for fulfilling compliance requirements and ensuring employees are following procedures.
• Plan, coordinate and implement projects requiring specialized experience. Make decisions within guidelines that impact immediate unit operations, such as inoculums preparation, bioreactor operation, centrifugation, protein purification, solution preparation, CIP/SIP unit operations, and troubleshooting and related production support operations.
• Assist in the implementation of new technology to achieve production goals. Identify and resolve potential cGMP issues and ensure compliance.
• Work with management on continuous operational improvement projects and oversee the progress within their area of responsibility.
• Distribute daily work assignments to leads and manufacturing technicians. Coach and train staff members in addition to identifying staff development needs in areas such as cGMP training, technical skills, safety, performance management, and best practices.
• Recommend and evaluate production efficiencies and organize the information to present to management for future projects.
• Ensure that all operations are performed with 100% compliance to SOPs and cGMP standards.

Benefits

• Relocation benefits are available for this posting.
• A discretionary annual bonus may be available based on individual and Company performance.
• This position also qualifies for the benefits detailed at the link provided below.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Professional, Scientific, and Technical Services
• Number of Employees: 5,001-10,000 employees